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FDA 510(k)

ULTEC THIN HYDROCOLLOID DRESSING

K-Number: K952071 · 1995-06-22

ApplicantSherwood Medical Co.
Decision Date1995-06-22
Product CodeMGP
DecisionSubstantially Equivalent

Device Summary

ULTEC THIN HYDROCOLLOID DRESSING is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Co.. It received FDA 510(k) clearance on 1995-06-22 under 510(k) number K952071. The device is classified under product code MGP. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ULTEC THIN HYDROCOLLOID DRESSING?

ULTEC THIN HYDROCOLLOID DRESSING is a medical device that received FDA 510(k) clearance on 1995-06-22. The listed applicant is Sherwood Medical Co.. The 510(k) number is K952071.

When did ULTEC THIN HYDROCOLLOID DRESSING receive FDA 510(k) clearance?

ULTEC THIN HYDROCOLLOID DRESSING received FDA 510(k) clearance on 1995-06-22, under 510(k) number K952071.

Who is the listed applicant for ULTEC THIN HYDROCOLLOID DRESSING?

The FDA 510(k) record lists Sherwood Medical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTEC THIN HYDROCOLLOID DRESSING?

The FDA product code for ULTEC THIN HYDROCOLLOID DRESSING is MGP.

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Other records listing Sherwood Medical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K981365MAHURKAR 13.5 FR CUFFED CATHETER WITH CURVED EXTENSIONSK960982MONOJECT BLUNT I.V. ACCESS CANNULA/MONOJECT HYPODERMIC SYRINGE WITH BLUNT I.V. ACCESS CANNULAK962880SENSI-TOUCH COMBO SPINAL/EPIDURAL REGIONAL ANESTHESIA DELIVERY SYSTEMK960574ARGYLE TURKEL NEONATAL/PEDIATRIC THORACIC CATHETER INSERTION TRAY AND THORACIC CATHETER SYSTEMK960677KANGAROO JEJUNAL FEEDING SYSTEMK960632KANGAROO FEEDING TUBE PLACMENT STYLET

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Related Devices (Code: MGP)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K012995COLLATEK SHEETBiocore Medical Technologies, Inc.K012997COLLATEK FOAMBiocore Medical Technologies, Inc.K001508LASERSKIN DRESSINGFidia Advanced Biopolymers SrlK990079FASTSEAL CHEST WOUND DRESSINGGreenfield Medical Technologies, Inc.K991214SIMPLICARE TRANSPARENT WOUND DRESSINGHollister, Inc.K992302DERMAPHYLYX SKIN PROTECTORS, PROTECT IT SKIN PROTECTORSDermaphylyx, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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